A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892673



Internal ID19183493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36242355..36279947hg38UCSC Ensembl
Outerchr15:36242355..36279947hg38UCSC Ensembl
Innerchr15:36534556..36572148hg19UCSC Ensembl
Outerchr15:36534556..36572148hg19UCSC Ensembl
Innerchr15:34321848..34359440hg18UCSC Ensembl
Outerchr15:34321848..34359440hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3837593
hg1937593
hg1837593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780231
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892673
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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